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Pseudo paralysis of the shoulder and increased C-reactive protein are predictive factors for septic shoulder in children superior to other clinical symptoms: a retrospective case series of 25 patients.

作者信息

Danilov Cezara, Ihle Christoph, Fernandez Francisco F, Blumenstock Gunnar, Wirth Thomas, Eberhardt Oliver

机构信息

Orthopaedic Department Olgahospital Stuttgart, Germany.

BG Trauma Center Tuebingen, Siegfried-Weller-Institute for Trauma Research, Eberhard-Karls-University, Tuebingen, Germany.

出版信息

J Child Orthop. 2020 Feb 1;14(1):85-90. doi: 10.1302/1863-2548.14.190126.

Abstract

PURPOSE

The aim of the study was to evaluate predictable parameters with the highest sensitivity used in the diagnosis of children septic shoulder arthritis.

METHODS

All children treated in our paediatric orthopaedic hospital between 2000 and 2017 with intraoperative verified septic arthritis of the shoulder were included in this retrospective study. Diagnostic procedures e.g. ultrasound, MRI, radiograph or blood samples as well as typical clinical symptoms were evaluated as predictable parameters for septic shoulder arthritis in paediatric patients. Descriptive statistics as well as sensitivity analysis were performed.

RESULTS

In all, 25 children, 20 boys and five girls, aged from eight days to 15 years, were included for further statistical analysis. All parameters included were tested for sensitivity with binomial confidence intervals (Cis) of 95%. Predictive parameters with highest sensitivity were pseudo paralysis (100%, CI 0.86 to 1.00) and C-reactive protein (CRP) (96%, CI 0.79 to 0.99) superior to temperature (52%, CI 0.3 to 0.73), white blood count (11%, CI 0.01 to 0.34), radiograph (21%, CI 0.04 to 0.50), ultrasound (71%, CI 0.47 to 0.88) or MRI (100%, CI 0.78 to 1.00).

CONCLUSION

The diagnosis of a septic arthritis of the shoulder in children can be challenging for the clinician and especially for the resident doctor. Clinical symptoms such as pseudo paralysis and increased CRP level must be considered as predictive markers not to delay further diagnostics and treatment.

LEVEL OF EVIDENCE

IV.

摘要

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